Fresenius Kabi Issues Critical Software Update for Ivenix Infusion Pumps
FDA identifies Class I recall as most serious type due to software anomalies that may cause unexpected shutdowns and interface freezing.
FDA identifies Class I recall as most serious type due to software anomalies that may cause unexpected shutdowns and interface freezing.
CMMS enhancements are designed to simplify healthcare organizations’ approach to Accreditation 360 and create inspection-ready documentation.
The latest Image Suite V4 release introduces AI-generated companion images, enhanced visualization tools, and workflow upgrades to support more confident diagnoses and a better user experience.
FDA identifies Class I recall as most serious type due to software anomalies that may cause unexpected shutdowns and interface freezing.
Blindly deploying vendor patches can sideline critical devices and jeopardize patient safety.
Read MoreThe solution converts standard non-contrast chest CTs into quantitative lung function maps and has also received CMS reimbursement confirmation.
Read MoreThe solutions are designed to streamline cardiac workflows and improve diagnostic confidence using artificial intelligence and automation.
Read MoreThe FDA-cleared, AI-guided software is now available on Butterfly Network’s handheld ultrasound devices, aiming to enable more healthcare professionals to perform cardiac exams.
Read MoreThe new system uses generative AI to detect sophisticated phishing and social engineering attacks that traditional filters may miss.
Read MoreHiLabs says the HITRUST i1 certification reinforces its commitment to data privacy and strengthens protections against evolving cybersecurity threats.
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The Authority to Operate status clears the platform for use in US Department of Defense medical facilities.